eyewash
Generic: eyewash
Labeler: global equipment companyDrug Facts
Product Profile
Brand Name
eyewash
Generic Name
eyewash
Labeler
global equipment company
Dosage Form
SOLUTION
Routes
Active Ingredients
water 465 mL/473mL
Manufacturer
Identifiers & Regulatory
Product NDC
78641-786
Product ID
78641-786_c4f783d3-b047-ab39-e053-2995a90ab6f3
Product Type
HUMAN OTC DRUG
Marketing Category
NDA
Application Number
NDA022305
Listing Expiration
2026-12-31
Marketing Start
2021-06-17
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
78641786
Hyphenated Format
78641-786
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
eyewash (source: ndc)
Generic Name
eyewash (source: ndc)
Application Number
NDA022305 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 465 mL/473mL
Packaging
- 473 mL in 1 BOTTLE, UNIT-DOSE (78641-786-67)
- 946 mL in 1 BOTTLE, UNIT-DOSE (78641-786-68)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "c4f783d3-b047-ab39-e053-2995a90ab6f3", "openfda": {"unii": ["059QF0KO0R"], "rxcui": ["1151101"], "spl_set_id": ["c4f78121-4668-2e0c-e053-2995a90ab6c6"], "manufacturer_name": ["Global Equipment Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, UNIT-DOSE (78641-786-67)", "package_ndc": "78641-786-67", "marketing_start_date": "20210617"}, {"sample": false, "description": "946 mL in 1 BOTTLE, UNIT-DOSE (78641-786-68)", "package_ndc": "78641-786-68", "marketing_start_date": "20210617"}], "brand_name": "Eyewash", "product_id": "78641-786_c4f783d3-b047-ab39-e053-2995a90ab6f3", "dosage_form": "SOLUTION", "product_ndc": "78641-786", "generic_name": "Eyewash", "labeler_name": "Global Equipment Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Eyewash", "active_ingredients": [{"name": "WATER", "strength": "465 mL/473mL"}], "application_number": "NDA022305", "marketing_category": "NDA", "marketing_start_date": "20210617", "listing_expiration_date": "20261231"}